A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2674



Internal ID15540433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:96836341..96854075hg38UCSC Ensembl
Outerchr7:96465653..96483387hg19UCSC Ensembl
Outerchr7:96303589..96321323hg18UCSC Ensembl
Outerchr7:96110304..96128038hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3817735
hg1917735
hg1817735
hg1717735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857
Supporting Variants
SamplesNA18555
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv2674
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer